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Epilepsy and phenylketonuria: a case description and EEG-fMRI findings
Phenylketonuria (PKU) is characterized by phenylalanine accumulation due to phenylalanine hydroxylase deficiency. Up to 50% of PKU patients experience seizures. We evaluated an adult PKU patient who suffered from absences and primarily generalized tonic-clonic seizures, associated with generalized s...
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| Autori principali: | , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
CIC Edizioni Internationali
2014
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4172251/ https://ncbi.nlm.nih.gov/pubmed/25014052 |
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